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Details

Autor(en) / Beteiligte
Titel
Risk of breast cancer two years after a benign biopsy depends on the mammographic feature prompting recall
Ist Teil von
  • Maturitas, 2021-02, Vol.144, p.53-59
Ort / Verlag
Ireland: Elsevier B.V
Erscheinungsjahr
2021
Quelle
MEDLINE
Beschreibungen/Notizen
  • •False-positive recalls with invasive assessments bear high-risk of breast cancer.•The risk is greater within two years after the recall.•The type of mammographic feature causing the recall influences breast cancer risk.•Cancers within two years after the recall are mostly diagnosed as interval cancers. We aimed to explore whether the type of mammographic feature prompting a false-positive recall (FPR) during mammography screening influences the risk and timing of breast cancer diagnosis, particularly if assessed with invasive procedures. We included information on women screened and recalled for further assessment in Spain between 1994 and 2015, with follow-up until 2017, categorizing FPRs by the assessment (noninvasive or invasive) and mammographic feature prompting the recall. Breast cancer rates in the first two years after FPR (first period) and after two years (second period). The study included 99,825 women with FPRs. In both periods, the breast cancer rate was higher in the invasive assessment group than in the noninvasive group (first period 12 ‰ vs 1.9 ‰, p < 0.001; second period 4.4‰ vs 3.1‰, p < 0.001). During the first period, the invasive assessment group showed diverse breast cancer rates for each type of mammographic feature, with a higher rate for asymmetric density (31.9‰). When the second period was compared with the first, the breast cancer rate decreased in the invasive assessment group (from 12‰ to 4.4‰, p < 0.001) and increased in the noninvasive assessment group (from 1.9‰ to 3.1‰, p < 0.001). In the context of mammography screening, the risk of breast cancer diagnosis during the first two years after FPR was particularly high for women undergoing invasive assessment; importantly, the risk was modified by type of mammographic feature prompting the recall. This information could help to individualize follow-up after exclusion of malignancy.

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